| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | IL17D, LOC130009328 (R80C +1 more) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | IL17D, LOC130009328 (C71S +1 more) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | IL17D, LOC130009328 (R27P +1 more) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | IL17D, LOC130009328 (P92L +1 more) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | IL17D, LOC130009328 (V50M +1 more) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | IL17D, LOC130009328 (A73P +1 more) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | IL17D, LOC130009328 (A33V +1 more) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | IL17D, LOC130009328 (A26T +1 more) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | IL17D, LOC130009328 (W94R +1 more) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (synonymous variant +2 more) | not provided | |
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